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Lazic

FDA UDI

Class II (US FDA UDI)

by Peter Lazic GmbH

Identity

Trade Name
LAZIC FDA UDI
Generic Name
Aneurysm clip FDA UDI
Device Name
D-Aneurysm STANDARD Clip TITANIUM permanent, slightly curved 11mm FDA UDI
Model / Reference
S.35.762 FDA UDI
Description
D-Aneurysm STANDARD Clip TITANIUM permanent, slightly curved 11mm FDA UDI

Identifiers

Catalog Number
S.35.762 FDA UDI
Primary DI / UDI-DI
04250603744382 FDA UDI
FDA Product Code
HCH FDA UDI
GMDN Term
Aneurysm clip FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Aneurysm clip

The LAZIC Aneurysm Clip is a permanent, slightly curved titanium device used to treat intracranial aneurysms and prevent bleeding from small blood vessels. Designed for implantation around the neck of an aneurysm, this device features a dedicated applier and comes with blades that open like jaws. With its approval by the FDA, this medical device is available in various sizes and is intended to be permanently implanted.

Similar devices

Also classified as Aneurysm clip.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Peter Lazic GmbH

Sources (1)

  • FDA UDI 2adb31cb-fb0f-41f6-a95b-b5c706a762b4 35 fields · synced Jul 24, 2026